D - Time
NDC Package 68210-1490-5

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

D - Time is uses temporarily relieves common cold/flu symptoms:cough due to minor throat and bronchial irritationsore throatheadacheminor aches and painsfevernasal congestion. Marketed by Spirit Pharmaceuticals,llc, this product is identified by NDC 68210-1490 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
68210-1490-5
Package Description
1 BAG in 1 DRUM / 5000 CAPSULE, LIQUID FILLED in 1 BAG
Product Code
68210-1490
11-Digit Billing Format
68210149005
RxNorm Crosswalk
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule

Clinical Specifications

Proprietary Name
D - Time
Dosage Form
-
Usage Information
Uses temporarily relieves common cold/flu symptoms:cough due to minor throat and bronchial irritationsore throatheadacheminor aches and painsfevernasal congestion

Regulatory & Marketing

Labeler Name
Spirit Pharmaceuticals,llc
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
05-30-2010
Listing Expiration
12-31-2018
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (68210-1490). Click a package code to view its specific billing and regulatory data.

68210-1490-4
1 BAG in 1 DRUM / 4000 CAPSULE, LIQUID FILLED in 1 BAG
68210-1490-6
1 BAG in 1 DRUM / 6000 CAPSULE, LIQUID FILLED in 1 BAG
68210-1490-8
1 BAG in 1 DRUM / 8000 CAPSULE, LIQUID FILLED in 1 BAG

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 68210-1490-5 identifies a specific commercial package of 1 bag in 1 drum / 5000 capsule, liquid filled in 1 bag of D - Time, labeled by Spirit Pharmaceuticals,llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Spirit Pharmaceuticals,llc on May 30, 2010. The current certification is valid through December 31, 2018.

How is this Spirit Pharmaceuticals,llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68210149005. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
68210-1490-5
11-Digit CMS (5-4-2)
68210-1490-05

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.